罕见头皮动静脉畸形的手术切除:病例报告。

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2024-09-24 eCollection Date: 2024-11-01 DOI:10.1097/MS9.0000000000002596
Khitamul Haq, Muhammad A Waqas, Saleem Akhter, Juan J Cardona, Gianluca Scalia, Giuseppe E Umana, Bipin Chaurasia
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引用次数: 0

摘要

导言和重要性:头皮动静脉畸形(AVM)是头皮动脉和静脉之间异常连接的复杂血管异常,会导致严重的并发症和美容问题。对于年轻女性患者来说,头皮动静脉畸形的治疗尤为复杂,其功能和美观效果都至关重要。本病例报告重点介绍了一名年轻女性头皮动静脉畸形患者的成功治疗,强调了早期诊断和多学科治疗的重要性:一名 30 岁的女性因头皮搏动性肿块和严重的外观问题前来就诊。超声波检查、脑部 CT 扫描、核磁共振成像和颈动脉 CT 血管造影等诊断性影像学检查证实患者患有头皮动静脉畸形。患者接受了综合治疗方案,首先进行血管内栓塞以减少动静脉畸形的血流量,然后进行手术切除以清除病灶。术后随访显示,患者的症状和病变体积明显减轻,未发现并发症:临床讨论:头皮动静脉畸形虽然罕见,但由于存在严重并发症(如出血和影响美观)的风险,因此需要及时诊断。在该病例中,超声波、CT 和核磁共振成像相结合,对 AVM 进行了详细评估。介入放射学和外科专家参与的多学科方法是成功的关键。血管内栓塞术最大限度地减少了术中出血,简化了手术切除,从而显著改善了症状和外观。持续监测对长期成功和早期发现复发至关重要:本病例强调了采用多学科方法治疗年轻女性头皮动静脉畸形的有效性。通过先进的成像技术进行早期诊断可实现及时和有针对性的干预。联合使用血管内栓塞术和手术切除术后,症状得到明显缓解,美观度也有所提高。专科医生之间的合作对于优化治疗效果至关重要,正在进行的研究将进一步完善治疗策略,提高头皮动静脉畸形患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical resection of a rare scalp arteriovenous malformation: a case report.

Introduction and importance: Scalp arteriovenous malformations (AVMs) are intricate vascular anomalies with abnormal connections between arteries and veins in the scalp, leading to serious complications and cosmetic concerns. Managing scalp AVMs is particularly complex in young female patients, where both functional and aesthetic outcomes are crucial. This case report highlights the successful treatment of a young woman with a scalp AVM, emphasizing the importance of early diagnosis and a multidisciplinary approach.

Case presentation: A 30-year-old female presented with a pulsatile scalp mass and significant cosmetic concerns. Diagnostic imaging, including ultrasonography, brain CT scan, MRI, and carotid CT angiogram, confirmed a scalp AVM. The patient underwent a comprehensive treatment plan beginning with endovascular embolization to reduce blood flow to the AVM, followed by surgical resection to remove the lesion. Postoperative follow-up showed a marked reduction in symptoms and lesion volume, with no complications observed.

Clinical discussion: Scalp AVMs, though rare, require prompt diagnosis due to the risk of severe complications such as hemorrhage and cosmetic impact. In this case, a combination of ultrasonography, CT, and MRI provided a detailed assessment of the AVM. A multidisciplinary approach, involving interventional radiology and surgical expertise, was crucial for success. Endovascular embolization minimized intraoperative bleeding and simplified surgical resection, leading to significant symptom and cosmetic improvements. Continuous monitoring is essential for long-term success and early detection of recurrences.

Conclusion: This case underscores the effectiveness of a multidisciplinary approach in managing scalp AVMs in young female patients. Early diagnosis through advanced imaging techniques enables timely and targeted intervention. The combined use of endovascular embolization and surgical resection led to significant symptom resolution and aesthetic enhancement. Collaboration among specialists is vital for optimizing outcomes, and ongoing research will further refine treatment strategies, improving the quality of life for patients with scalp AVMs.

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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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